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家族性原发性淀粉样变性的荧光造影结果。

Fluorographical findings in familial primary amyloidosis.

作者信息

Tsukahara S, Matsuo T

出版信息

Ophthalmologica. 1978;176(6):301-7. doi: 10.1159/000308721.

Abstract

A 50-year-old man, diagnosed as having familial primary amyloidosis due to his systemic symptoms, family history, and to histological examination of biopsy specimens, was examined by fluorescein angiography. The following results were obtained: (1) The sheathing retinal artery showed a defect of dye filling in one region, but not in the other region. Dye leakage from the sheathing artery was observed. (2) The configuration of macular vessels was rough, a microaneurysma-like change and the leakage of dye were also recognized in the capillaries of this region. (3) It was speculated that vitreous opacity originated from vascular lesions.

摘要

一名50岁男性,因其全身症状、家族病史以及活检标本的组织学检查被诊断为家族性原发性淀粉样变性,接受了荧光素血管造影检查。结果如下:(1)视网膜动脉鞘在一个区域显示染料充盈缺损,而在另一个区域则未显示。观察到染料从动脉鞘渗漏。(2)黄斑血管形态粗糙,该区域的毛细血管也出现了类似微动脉瘤的变化以及染料渗漏。(3)推测玻璃体混浊源于血管病变。

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